CN1562879A - High-strength and high-toughness zirconia-based ceramic and preparation method thereof - Google Patents
High-strength and high-toughness zirconia-based ceramic and preparation method thereof Download PDFInfo
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- CN1562879A CN1562879A CN 200410029886 CN200410029886A CN1562879A CN 1562879 A CN1562879 A CN 1562879A CN 200410029886 CN200410029886 CN 200410029886 CN 200410029886 A CN200410029886 A CN 200410029886A CN 1562879 A CN1562879 A CN 1562879A
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- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 title claims abstract description 53
- 238000002360 preparation method Methods 0.000 title claims abstract description 34
- 239000000919 ceramic Substances 0.000 title claims abstract description 22
- 239000000843 powder Substances 0.000 claims abstract description 52
- 239000002131 composite material Substances 0.000 claims abstract description 21
- RKTYLMNFRDHKIL-UHFFFAOYSA-N copper;5,10,15,20-tetraphenylporphyrin-22,24-diide Chemical compound [Cu+2].C1=CC(C(=C2C=CC([N-]2)=C(C=2C=CC=CC=2)C=2C=CC(N=2)=C(C=2C=CC=CC=2)C2=CC=C3[N-]2)C=2C=CC=CC=2)=NC1=C3C1=CC=CC=C1 RKTYLMNFRDHKIL-UHFFFAOYSA-N 0.000 claims abstract description 20
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims abstract description 17
- 229910001928 zirconium oxide Inorganic materials 0.000 claims abstract description 17
- 239000002002 slurry Substances 0.000 claims abstract description 16
- VCRLKNZXFXIDSC-UHFFFAOYSA-N aluminum oxygen(2-) zirconium(4+) Chemical compound [O--].[O--].[Al+3].[Zr+4] VCRLKNZXFXIDSC-UHFFFAOYSA-N 0.000 claims abstract description 12
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims abstract description 10
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 10
- 238000005266 casting Methods 0.000 claims abstract description 8
- SIWVEOZUMHYXCS-UHFFFAOYSA-N oxo(oxoyttriooxy)yttrium Chemical compound O=[Y]O[Y]=O SIWVEOZUMHYXCS-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000002994 raw material Substances 0.000 claims abstract description 8
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims abstract description 6
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims abstract description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 16
- 238000009413 insulation Methods 0.000 claims description 14
- 239000002245 particle Substances 0.000 claims description 14
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 11
- 239000007864 aqueous solution Substances 0.000 claims description 10
- 239000007788 liquid Substances 0.000 claims description 10
- 239000011230 binding agent Substances 0.000 claims description 9
- 239000006185 dispersion Substances 0.000 claims description 8
- 229910000329 aluminium sulfate Inorganic materials 0.000 claims description 7
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical group [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 claims description 7
- 238000001035 drying Methods 0.000 claims description 6
- 239000011259 mixed solution Substances 0.000 claims description 6
- 238000003756 stirring Methods 0.000 claims description 6
- 238000010792 warming Methods 0.000 claims description 5
- 238000013019 agitation Methods 0.000 claims description 4
- 235000011114 ammonium hydroxide Nutrition 0.000 claims description 4
- 235000011194 food seasoning agent Nutrition 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 230000007935 neutral effect Effects 0.000 claims description 4
- 238000000967 suction filtration Methods 0.000 claims description 4
- 239000000725 suspension Substances 0.000 claims description 4
- 238000005406 washing Methods 0.000 claims description 4
- 159000000013 aluminium salts Chemical class 0.000 claims description 3
- 238000007872 degassing Methods 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- 229910021502 aluminium hydroxide Inorganic materials 0.000 claims description 2
- ATYZRBBOXUWECY-UHFFFAOYSA-N zirconium;hydrate Chemical compound O.[Zr] ATYZRBBOXUWECY-UHFFFAOYSA-N 0.000 claims description 2
- 239000004160 Ammonium persulphate Substances 0.000 claims 1
- 235000019395 ammonium persulphate Nutrition 0.000 claims 1
- 229920000058 polyacrylate Polymers 0.000 claims 1
- 238000005516 engineering process Methods 0.000 abstract description 8
- 238000005245 sintering Methods 0.000 abstract description 8
- 239000013078 crystal Substances 0.000 abstract description 4
- 239000011248 coating agent Substances 0.000 abstract 2
- 238000000576 coating method Methods 0.000 abstract 2
- 239000003431 cross linking reagent Substances 0.000 abstract 1
- 239000002270 dispersing agent Substances 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 239000002585 base Substances 0.000 description 10
- 239000000047 product Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000001272 pressureless sintering Methods 0.000 description 4
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000001179 sorption measurement Methods 0.000 description 3
- 238000007669 thermal treatment Methods 0.000 description 3
- 229910052684 Cerium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- -1 silicon nitrides Chemical class 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 238000004448 titration Methods 0.000 description 2
- 229910052727 yttrium Inorganic materials 0.000 description 2
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 2
- DUNKXUFBGCUVQW-UHFFFAOYSA-J zirconium tetrachloride Chemical compound Cl[Zr](Cl)(Cl)Cl DUNKXUFBGCUVQW-UHFFFAOYSA-J 0.000 description 2
- BNGXYYYYKUGPPF-UHFFFAOYSA-M (3-methylphenyl)methyl-triphenylphosphanium;chloride Chemical compound [Cl-].CC1=CC=CC(C[P+](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 BNGXYYYYKUGPPF-UHFFFAOYSA-M 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 238000000975 co-precipitation Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000011858 nanopowder Substances 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000012716 precipitator Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
Landscapes
- Compositions Of Oxide Ceramics (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Abstract
The invention discloses a high-strength high-toughness ceramic and a preparation method thereof. The invention solves the problems of lower toughness of zirconia-based ceramic prepared by the existing normal pressure sintering technology and difficult preparation of high-concentration and low-viscosity slurry during wet forming. Coating aluminum hydroxide on nano-oxideAnd performing heat treatment on the surface of zirconium (containing 4.37-6.04% of yttrium oxide) powder to form zirconium oxide-aluminum oxide composite micro powder (the content of tetragonal zirconium oxide in the micro powder accounts for 70-90% of the total amount of zirconium oxide). The composite micro powder, acrylamide, a cross-linking agent and a dispersing agent are used as raw materials, green bodies are prepared through gel casting, and the ceramic is prepared under the condition of normal pressure sintering, wherein the strength is 700-1000 MPa, and the toughness is 15-17 MPa.m1/2. The invention takes the composite powder of the coating of the nanometer zirconia powder by the alumina and the organic combination as the raw material, combines and uses the advanced gel-casting technology to prepare the green compact with uniform structure, and prepares the fine-grained high-strength high-toughness ceramic by the effective inhibition of the growth of zirconia crystal grains by the alumina layer coated on the surface at high temperature.
Description
Technical field
The present invention relates to a kind of pottery and preparation method thereof, specifically, the present invention relates to a kind of high-intensity high-tenacity zirconia-based ceramics and preparation method thereof.
Background technology
High-performance zirconia must adopt fine powder and suitable Technology.At present, quality oxide zirconium based ceramic powder material is by the preparation of basic zirconium chloride (the water-soluble salt that contains yttrium or the cerium) precipitator method, is prepared into the zirconium white powder through thermal treatment then.Between the 30-100 nanometer, tetragonal phase zirconium oxide content is fit to dry-press process through granulation about 50% by the powder particle size of this method preparation, and the ceramics strength of its pressureless sintering is at 600～800MPa, and fracture toughness property is at 10～12MPam
1/2Perhaps use coprecipitation method preparations such as basic zirconium chloride (the water-soluble salt that contains yttrium or cerium) and aluminum soluble salt, be prepared into zirconium white and aluminum oxide composite powder through thermal treatment then, ceramic performance dry-pressing formed, pressureless sintering is better than preceding a kind of method.The high tenacity pottery requires crystal grain tiny, the second phase crystal grain is close with basic grain size, usually must adopt special production technique (as sintering hot pressing) just can reach above-mentioned requirements, as preparing ceramics strength at 1000～1600MPa with hot pressed sintering, fracture toughness property is at 14～18MPam
1/2, but production cost height can not be made the product of complicated shape.Utilize second to strengthen flexible nano ceramics technology mutually and increased substantially the strength of materials in recent years, but toughness of material is not significantly increased, and will uses Fast Sintering equipment, can not make the product of complicated shape.The nineties in last century, the development of ceramic wet forming technique is rapid, and the stupalith for preparing complicated shape for low cost has been established the technology basis.One of its gordian technique is preparation high density, low viscous slurry.With the gel-casting technology is example, and this processing unit is simple, and the blank density height of moulding, intensity is big, shrinking percentage is less, and ceramic product reliability height is with existing more research of pottery and application such as the aluminum oxide of this method preparation and silicon nitrides.But because high-performance zirconia base pottery uses nanopowder, high density, low viscous pulp preparation difficulty, relevant research is less.
The nano zircite powder is owing to its bigger specific surface area, and the surface adsorption water yield is big, and gathering makes the zirconium white grain growth easily, when granularity increases, has reduced the content of tetragonal phase zirconium oxide.When adopting 30～70nm zirconium white powder as raw material at present, the volume fraction maximum of zirconium white powder can only reach 25～28% during the preparation low viscosity slurry, can not satisfy the requirement that wet moulding prepares high-performance ceramic.
Summary of the invention
The present invention for the production cost height that solves in the prior art preparation high-performance zirconia base pottery and exist, can not prepare the problem of complex-shaped product and high density, low viscosity slurry preparation difficulty, high-intensity high-tenacity zirconia-based ceramics of the present invention and preparation method thereof is proposed.
High-intensity high-tenacity zirconia-based ceramics of the present invention is mainly annotated the type method of congealing into and is made by high tetragonal phase zirconium oxide-aluminum oxide composite powder employing.
The described high tetragonal phase zirconium oxide-preferred alumina-coated powdered zirconium oxide of aluminum oxide composite powder surface, wherein tetragonal phase zirconium oxide content accounts for the 70-90% of zirconium white total amount.
Described high tetragonal phase zirconium oxide-further preferable particle size of aluminum oxide composite powder is 100～200nm, is made up of the component that comprises following weight per-cent: zirconium white 74～96%, yttrium oxide 2～6%, aluminum oxide 2～20%.
Described high tetragonal phase zirconium oxide-aluminum oxide composite powder is preferably made by following preparation method:
(1) raw material powdered zirconium oxide and water are made into suspension according to weight ratio 1: 1～3 mixing stirrings; It is 20～60% the aqueous solution that aluminium salt is made into weight percent concentration; The two is mixed stirring obtain zirconium white-aluminium salt mixed solution; Described raw material zirconium white fine powder particle diameter is 30～70nm, contains weight percent 4.37～6.04% yttrium oxide;
(2) under agitation, ammoniacal liquor slowly being splashed in zirconium white-aluminium salt mixed solution that step (2) obtains, is 8～10 until the pH of mixed solution value, and is to keep 0～2 hour under 8～10 the condition in the pH value, filters, and washing is to neutral, and suction filtration obtains powder;
(3) the powder drying that step (2) is obtained is heat-treated then and is made the aluminium hydroxide that is coated on the powdered zirconium oxide surface be decomposed into aluminum oxide, obtains the Zirconia-alumina composite powder of high cubic phase.
The preferred aluminum chloride of described aluminium salt or its hydrate, aluminum nitrate or its hydrate, Tai-Ace S 150 or its hydrate, two or more mixture in them.
Described particle diameter is that the raw material powdered zirconium oxide that contains 4.37～6.04% yttrium oxide of 30～70nm is a market product.
Described heat treating method preferably kept 0.5～3 hour under 900～1200 ℃ of temperature.The heat-up rate that is more preferably with 100 ℃/h is warming up to 200～300 ℃, keeps 0～2 hour at 200～300 ℃, rises to 900～1200 ℃ and kept 0.5～3 hour with same heat-up rate then.The water yield and the crystal water of surface adsorption can be removed the generation aluminum oxide down at 200～300 ℃, under 900～1200 ℃, aluminum oxide and zirconium white be formed composition particles.
The preparation method of high-intensity high-tenacity pottery of the present invention may further comprise the steps:
(1) acrylamide, linking agent being made into weight percent by weight 20: 1 is 14% water base premixed liquid;
(2) the water base premixed liquid with high tetragonal phase zirconium oxide-aluminum oxide composite powder, dispersion agent and step (1) mixes according to weight ratio 100: 1～1.8: 25～28, grinds and makes slurry;
(3) slurry that step (2) is obtained vacuumizes the aqueous solution that adds solidifying agent after the degasification, slurry and weight percent are that the weight ratio of 1% aqueous solution of curing agent is 100: 0.5～1, casting at room temperature, solidify down at 60～80 ℃, dry back pre-burning binder removal, descended normal pressure-sintered 1～3 hour at 1500～1700 ℃ then, obtain pottery of the present invention.
Described solidifying agent initiator system of ammonium persulfate.
The preferred N of described linking agent, the N-methylene diacrylamine, described dispersion agent optimization polypropylene acid ammonium,
In ceramic preparation, dry preferred described in the step (3) under the condition of relative humidity 70～90% dry 12～36 hours, and then seasoning.Described pre-burning binder removal is preferably: heat-up rate is 100 ℃/h, 300 ℃ of insulations 0.5 hour, 500 ℃ of insulations 0.5 hour, 900 ℃ of insulations 0.5 hour.Described sintering is preferably: heat-up rate is 100～150 ℃/h, is warming up to 1500～1700 ℃ of insulations 1～3 hour.
The present invention uses wet method injectiong coagulation shaping technology and pressureless sintering method just can obtain the high-intensity high-tenacity pottery, and processing method is simple, and production cost is low, is easy to prepare the complicated product of shape.The ceramics strength of preparation is 700～1000MPa, and toughness reaches 15～17MPam
1/2
The present invention utilizes the powder that coats one deck alumina layer in zirconium surface.Because outer oxide aluminium produces effect of contraction to the internal layer zirconium white, improved the cubic phase content of zirconium white powder, the utilization ratio of zirconium white powder is improved.The cubic phase content of untreated zirconium white powder is about 51% o'clock of total zirconium white amount, and cubic phase content is about 80% of total zirconium white amount in the powder of utilization of the present invention.Simultaneous oxidation aluminium-zirconia particles increases through the thermal treatment granularity, when the particle diameter of untreated zirconium white powder is about 30～50nm, the powder particle size of utilization of the present invention is increased to 100～200nm, reduced the surface adsorption water yield, it is electrical that aluminum oxide has changed zirconium surface, thereby improved the consistency with dispersion agent.Can reach 37～40% by solid volume fraction in the low viscosity slurry of powder preparation of the present invention, and overcome the shortcoming of annotating body drying condition strictness when congealing into type preparation pottery, coat one deck alumina layer simultaneously and suppressed zirconium white grain growth under the high temperature effectively, form the fine crystalline structure of complex phase ceramic, the cubic phase content of zirconium white powder increases, the notes type that congeals into makes green structure even, thereby make the ceramic sintered bodies even structure, pressureless sintering can obtain the pottery of high-toughness high-strength, intensity is 700～1000MPa, and toughness reaches 15～17MPam
1/2
Embodiment
Adopt the mode of embodiment to further specify high-intensity high-tenacity pottery of the present invention and preparation method thereof below, but the present invention is not limited to these embodiment.
Embodiment 1
(1) prepare high tetragonal phase zirconium oxide-aluminum oxide composite powder powder:
With particle diameter is that the powdered zirconium oxide 100g of 30～50nm joins to stir in the 200g water and is mixed with suspension; Al (NO with 36.76g
3)
310H
2It is 20% the aqueous solution that O is made into mass percent concentration: with the two mixing, and slow titration ammoniacal liquor under agitation, the pH value slowly is adjusted to 8～10, Al (NO in this process from 3～4
3)
3Generate Al (OH)
3Homogeneously precipitate in zirconic surface, keep the pH value at 8～10 times 1 hour, filter, the washing powder is to neutral, heat-treat after suction filtration, the drying, heat-up rate is 100 ℃/h, 280 ℃ of insulations 0.5 hour, continues to be warming up to 1050 ℃ then, be incubated 2 hours, obtain high tetragonal phase zirconium oxide of the present invention-aluminum oxide composite powder, particle diameter is 100～200nm, and cubic phase content accounts for 75～80% of zirconium white total amount; The zirconia content that contains 5.21% yttrium oxide is 95%, and alumina content is 5%.
(2) preparation high-intensity high-tenacity pottery of the present invention
With acrylamide, N, the N-methylene diacrylamine was made into 14% water base premixed liquid by weight 20: 1.In the powder 100g of preparation, add water base premixed liquid of 20g and 1.8g dispersion agent and make slurry with the planetary mills grinding, the ammonium persulfate solution 0.8g that adds concentration expressed in percentage by weight 1% after the vacuum stripping, casting at room temperature, solidify down at 70 ℃, after under the condition of relative humidity 70～90% dry 24 hours, seasoning, then 0.5 hour, 500 ℃ insulations of 300 ℃ of insulations 0.5 hour, under 0.5 hour systems of 900 ℃ of insulations the pre-burning binder removal.Base substrate heats up with 100 ℃/h of heat-up rate behind the binder removal, 1600 ℃ of following sintering 2 hours, obtains pottery of the present invention, and intensity is 827MPa, and toughness is 15.9MPam
1/2
Embodiment 2
(1) prepare high tetragonal phase zirconium oxide-aluminum oxide composite powder powder:
With particle diameter is that the powdered zirconium oxide 100g of 50nm joins to stir in the 150g water and is mixed with suspension; AlCl with 94.7g
36H
2It is 40% the aqueous solution that O is made into mass percent concentration; With the two mixing, under agitation slow titration ammoniacal liquor, the pH value slowly is adjusted to 8～10, AlCl in this process
3Generate Al (OH)
3Homogeneously precipitate in zirconic surface, keep the pH value at 8～10 times 1 hour, filter, the washing powder is to neutral, heat-treat after suction filtration, the drying, heat-up rate is 100 ℃/h, 280 ℃ of insulations 0.5 hour, continues to be warming up to 1050 ℃ then, be incubated 2 hours, obtain high tetragonal phase zirconium oxide of the present invention-aluminum oxide composite powder, particle diameter is 100～200nm, and cubic phase content accounts for 75～80% of zirconium white total amount; The zirconia content that contains 5.21% yttrium oxide is 80%, and alumina content is 20%.
(2) preparation high-intensity high-tenacity pottery of the present invention
With acrylamide, N, the N-methylene diacrylamine was made into 14% water base premixed liquid by weight 20: 1.In the powder 100g of preparation, add water base premixed liquid of 20g and 1.8g dispersion agent and make slurry with the planetary mills grinding, the ammonium persulfate solution 0.8g that adds concentration expressed in percentage by weight 1% after the vacuum stripping, casting at room temperature, solidify down at 70 ℃, after under the condition of relative humidity 70～90% dry 24 hours, seasoning is then by being incubated 0.5 hour 300,500 ℃ are incubated 0.5 hour, pre-burning binder removal under 0.5 hour systems of 900 ℃ of insulations.Base substrate heats up with 100 ℃/h of heat-up rate behind the binder removal, 1600 ℃ of following sintering 2 hours, obtains pottery of the present invention, and intensity is 710MPa, and toughness is 16.6MPam
1/2
Claims (10)
1. high-intensity high-tenacity zirconia-based ceramics is characterized in that it is mainly adopted by high tetragonal phase zirconium oxide-aluminum oxide composite powder to annotate the type method of congealing into and make.
2. pottery according to claim 1, it is characterized in that described high tetragonal phase zirconium oxide-aluminum oxide composite powder be alumina-coated on the powdered zirconium oxide surface, and tetragonal phase zirconium oxide content accounts for the 70-90% of total zirconia content.
3. pottery according to claim 2, the particle diameter that it is characterized in that described high tetragonal phase zirconium oxide-aluminum oxide composite powder is 100～200nm, form by the component that comprises following weight per-cent: zirconium white 74～96%, yttrium oxide 2～6%, aluminum oxide 2～20%.
4. pottery according to claim 1 is characterized in that described high tetragonal phase zirconium oxide-aluminum oxide composite powder made by following preparation method:
(1) raw material powdered zirconium oxide and water are made into suspension according to weight ratio 1: 1～3 mixing stirrings; It is 20～60% the aqueous solution that aluminium salt is made into weight percent concentration; The two is mixed stirring obtain zirconium white-aluminium salt mixed solution; Described raw material zirconium white fine powder particle diameter is 30～70nm, contains weight percent 4.37～6.04% yttrium oxide;
(2) under agitation, ammoniacal liquor slowly being splashed in zirconium white-aluminium salt mixed solution that step (2) obtains, is 8～10 until the pH of mixed solution value, and is to keep 0～2 hour under 8～10 the condition in the pH value, filters, and washing is to neutral, and suction filtration obtains powder;
(3) the powder drying that step (2) is obtained is heat-treated then and is made the aluminium hydroxide that is coated on the powdered zirconium oxide surface be decomposed into aluminum oxide, obtains the Zirconia-alumina composite powder of high cubic phase.
5. pottery according to claim 1 is characterized in that it is made by following preparation method:
(1) acrylamide, linking agent being made into weight percent by weight 20: 1 is 14% water base premixed liquid;
(2) the water base premixed liquid with high tetragonal phase zirconium oxide-aluminum oxide composite powder, dispersion agent and step (1) mixes according to weight ratio 100: 1～1.8: 25～28, grinds and makes slurry;
(3) slurry that step (2) is obtained vacuumizes the aqueous solution that adds solidifying agent after the degasification, slurry and weight percent are that the weight ratio of 1% aqueous solution of curing agent is 100: 0.5～1, casting at room temperature, solidify down at 60～80 ℃, dry back back pre-burning binder removal, descended normal pressure-sintered 1～3 hour at 1500～1700 ℃ then, obtain pottery of the present invention.
6. the preparation method of the described pottery of claim 1 is characterized in that it may further comprise the steps:
(1) acrylamide, linking agent being made into weight percent by weight 20: 1 is 14% water base premixed liquid;
(2) the water base premixed liquid with high tetragonal phase zirconium oxide-aluminum oxide composite powder, dispersion agent and step (1) mixes according to weight ratio 100: 1～1.8: 25～28, grinds and makes slurry;
(3) slurry that step (2) is obtained vacuumizes the aqueous solution that adds solidifying agent after the degasification, slurry and weight percent are that the weight ratio of 1% aqueous solution of curing agent is 100: 0.5～1, casting at room temperature, solidify down at 60～80 ℃, dry back pre-burning binder removal, descended normal pressure-sintered 1～3 hour at 1500～1700 ℃ then, obtain pottery of the present invention.
7. preparation method according to claim 6 is characterized in that described linking agent is N, and N-methylene diacrylamine, described dispersion agent are ammonium polyacrylate, and described solidifying agent is an ammonium persulphate.
8. preparation method according to claim 6 is characterized in that the drying described in the step (3) under the condition of relative humidity 70～90% dry 12～36 hours, and then seasoning.
9. preparation method according to claim 6, it is characterized in that the pre-burning binder removal described in the step (3) is: heat-up rate is 100 ℃/h, 300 ℃ of insulations 0.5 hour, 500 ℃ of insulations 0.5 hour, 900 ℃ of insulations 0.5 hour.
10. preparation method according to claim 6, it is characterized in that being sintered to described in the step (3): heat-up rate is 100～150 ℃/h, is warming up to 1500～1700 ℃ of insulations 1～3 hour.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200410029886 CN1260173C (en) | 2004-03-31 | 2004-03-31 | High-strength and high-toughness zirconia-based ceramic and preparation method thereof |
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Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1321089C (en) * | 2005-11-21 | 2007-06-13 | 天津大学 | Zirconium oxide base complex phase ceramic and preparation process thereof |
| CN100560534C (en) * | 2007-06-19 | 2009-11-18 | 西安交通大学 | A kind of manufacture method of alumina based ceramic core |
| CN103172385A (en) * | 2013-04-11 | 2013-06-26 | 成都科宁达材料有限公司 | Preparation method of 3mol percent yttria stabilized tetragonal phase zirconia polycrystalline (3Y-TZP) for teeth |
| CN104402226A (en) * | 2014-10-31 | 2015-03-11 | 三祥新材股份有限公司 | Zirconium based high temperature resistant composite ceramic coating preparation method |
| CN105479500A (en) * | 2016-01-21 | 2016-04-13 | 东莞市罗曼罗兰电器科技有限公司 | Ceramic shaver cutter |
| CN109896856A (en) * | 2019-04-12 | 2019-06-18 | 南京航空航天大学 | A kind of zirconia-based ceramics and its preparation method and application |
| CN112430114A (en) * | 2020-11-04 | 2021-03-02 | 湖南精城特种陶瓷有限公司 | Zirconium-aluminum composite nano ceramic and preparation method thereof |
| WO2021132315A1 (en) * | 2019-12-24 | 2021-07-01 | 関東電化工業株式会社 | Coated zirconia microparticle and method for producing same |
| JP2023513812A (en) * | 2020-02-17 | 2023-04-03 | インスティテュート ストローマン アーゲー | Glass-ceramic and its manufacturing method |
| CN116751077A (en) * | 2023-06-28 | 2023-09-15 | 浙江大学 | Method for preparing alumina micro-nano structural layer on zirconia surface based on secondary precipitation-heat treatment, product and application thereof |
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2004
- 2004-03-31 CN CN 200410029886 patent/CN1260173C/en not_active Expired - Fee Related
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1321089C (en) * | 2005-11-21 | 2007-06-13 | 天津大学 | Zirconium oxide base complex phase ceramic and preparation process thereof |
| CN100560534C (en) * | 2007-06-19 | 2009-11-18 | 西安交通大学 | A kind of manufacture method of alumina based ceramic core |
| CN103172385A (en) * | 2013-04-11 | 2013-06-26 | 成都科宁达材料有限公司 | Preparation method of 3mol percent yttria stabilized tetragonal phase zirconia polycrystalline (3Y-TZP) for teeth |
| CN103172385B (en) * | 2013-04-11 | 2014-12-10 | 成都科宁达材料有限公司 | Preparation method of 3mol percent yttria stabilized tetragonal phase zirconia polycrystalline (3Y-TZP) for teeth |
| CN104402226A (en) * | 2014-10-31 | 2015-03-11 | 三祥新材股份有限公司 | Zirconium based high temperature resistant composite ceramic coating preparation method |
| CN105479500A (en) * | 2016-01-21 | 2016-04-13 | 东莞市罗曼罗兰电器科技有限公司 | Ceramic shaver cutter |
| CN109896856A (en) * | 2019-04-12 | 2019-06-18 | 南京航空航天大学 | A kind of zirconia-based ceramics and its preparation method and application |
| WO2021132315A1 (en) * | 2019-12-24 | 2021-07-01 | 関東電化工業株式会社 | Coated zirconia microparticle and method for producing same |
| CN114829304A (en) * | 2019-12-24 | 2022-07-29 | 关东电化工业株式会社 | Coated zirconia fine particles and method for producing same |
| JP2023513812A (en) * | 2020-02-17 | 2023-04-03 | インスティテュート ストローマン アーゲー | Glass-ceramic and its manufacturing method |
| CN112430114A (en) * | 2020-11-04 | 2021-03-02 | 湖南精城特种陶瓷有限公司 | Zirconium-aluminum composite nano ceramic and preparation method thereof |
| CN116751077A (en) * | 2023-06-28 | 2023-09-15 | 浙江大学 | Method for preparing alumina micro-nano structural layer on zirconia surface based on secondary precipitation-heat treatment, product and application thereof |
| CN116751077B (en) * | 2023-06-28 | 2024-05-14 | 浙江大学 | Method for preparing alumina micro-nano structural layer on zirconia surface based on secondary precipitation-heat treatment, product and application thereof |
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